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遗传学研究中严重且持久的神经性厌食症表型纳入:一项范围综述

Inclusion of the severe and enduring anorexia nervosa phenotype in genetics research: a scoping review.

作者信息

Ramsay Sarah, Allison Kendra, Temples Heide S, Boccuto Luigi, Sarasua Sara M

机构信息

Healthcare Genetics and Genomics Program, School of Nursing, Clemson University, Clemson, SC 29634, USA.

School of Nursing, Clemson University , Clemson, SC 29634, USA.

出版信息

J Eat Disord. 2024 Apr 29;12(1):53. doi: 10.1186/s40337-024-01009-9.

Abstract

BACKGROUND

Anorexia nervosa has one of the highest mortality rates of all mental illnesses. For those who survive, less than 70% fully recover, with many going on to develop a more severe and enduring phenotype. Research now suggests that genetics plays a role in the development and persistence of anorexia nervosa. Inclusion of participants with more severe and enduring illness in genetics studies of anorexia nervosa is critical.

OBJECTIVE

The primary goal of this review was to assess the inclusion of participants meeting the criteria for the severe enduring anorexia nervosa phenotype in genetics research by (1) identifying the most widely used defining criteria for severe enduring anorexia nervosa and (2) performing a review of the genetics literature to assess the inclusion of participants meeting the identified criteria.

METHODS

Searches of the genetics literature from 2012 to 2023 were performed in the PubMed, PsycINFO, and Web of Science databases. Publications were selected per the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR). The criteria used to define the severe and enduring anorexia nervosa phenotype were derived by how often they were used in the literature since 2017. The publications identified through the literature search were then assessed for inclusion of participants meeting these criteria.

RESULTS

most prevalent criteria used to define severe enduring anorexia nervosa in the literature were an illness duration of ≥ 7 years, lack of positive response to at least two previous evidence-based treatments, a body mass index meeting the Diagnostic and Statistical Manual of Mental Disorders-5 for extreme anorexia nervosa, and an assessment of psychological and/or behavioral severity indicating a significant impact on quality of life. There was a lack of consistent identification and inclusion of those meeting the criteria for severe enduring anorexia nervosa in the genetics literature.

DISCUSSION

This lack of consistent identification and inclusion of patients with severe enduring anorexia nervosa in genetics research has the potential to hamper the isolation of risk loci and the development of new, more effective treatment options for patients with anorexia nervosa.

摘要

背景

神经性厌食症是所有精神疾病中死亡率最高的疾病之一。对于那些存活下来的患者,不到70%能完全康复,许多人会发展出更严重、更持久的症状表现。现在的研究表明,基因在神经性厌食症的发生和持续存在中起作用。在神经性厌食症的基因研究中纳入患有更严重、更持久疾病的参与者至关重要。

目的

本综述的主要目标是通过(1)确定严重持久神经性厌食症最广泛使用的定义标准,以及(2)对基因文献进行综述以评估符合已确定标准的参与者的纳入情况,来评估基因研究中符合严重持久神经性厌食症标准的参与者的纳入情况。

方法

在PubMed、PsycINFO和Web of Science数据库中对2012年至2023年的基因文献进行检索。根据系统评价和Meta分析扩展版的范围综述的首选报告项目(PRISMA-ScR)选择出版物。用于定义严重持久神经性厌食症表型的标准是根据自2017年以来在文献中的使用频率得出的。然后评估通过文献检索确定的出版物中是否纳入了符合这些标准的参与者。

结果

文献中用于定义严重持久神经性厌食症最普遍的标准是病程≥7年、对至少两种先前基于证据的治疗无阳性反应、体重指数符合《精神疾病诊断与统计手册》第5版中极端神经性厌食症的标准,以及心理和/或行为严重程度评估表明对生活质量有重大影响。基因文献中缺乏对符合严重持久神经性厌食症标准者的一致识别和纳入。

讨论

基因研究中对严重持久神经性厌食症患者缺乏一致的识别和纳入,有可能阻碍风险基因座的分离以及为神经性厌食症患者开发新的、更有效的治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a18d/11059621/acbb3a8e7338/40337_2024_1009_Fig1_HTML.jpg

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